Single crystals of the title salt, (C(3)H(10)N(3))(2)[Sn(CH(3))(2)(H(2)O)(4)](SO(4))(2), formed concomitantly with the already known [Sn(CH(3))(3)](2)SO(4)·2H(2)O. In the title structure, the Sn(IV) atom displays a slightly distorted octa-hedral coordination geometry defined by four O water atoms in the equatorial positions and two methyl groups in the axial positions. In the crystal, various O-H⋯O and N-H⋯O hydrogen-bonding inter-actions between the organic cation and the coordinated water mol-ecules as donors and the sulfate O atoms as acceptors result in a three-dimensional structure. The Sn(IV) atom is located on an inversion centre, resulting in half of the complex metal cation being in the asymmetric unit.
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http://dx.doi.org/10.1107/S1600536811053761 | DOI Listing |
Chemistry
December 2024
Department of Chemistry, Faculty of Science, Niigata University, Nishi-ku, Niigata, 950-2181, Japan.
Porphyrinoids in the 20π-electron state have been extensively studied from the fundamental viewpoint of investigating their structure-antiaromaticity relationships. However, most of the 20π porphyrinoids are highly distorted and unstable in air, which hinder the comprehensive analysis of paratropic ring-current effects derived from planar π-electron systems. Herein, we present the first examples of antiaromatic Sn(IV) complexes of 5,10,15,20-tetraaryl-5,15-diazaporphyrinoids (SnXTADAPs), prepared by the complexation of the corresponding freebases with Sn(II) chloride under aerobic conditions and subsequent metathesis of the axial ligands, that show paratropic ring-current effects.
View Article and Find Full Text PDFChem Asian J
November 2024
Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, 247667, India.
Sn(IV) complex of N-Confused Porphyrin (Sn(IV)-NCP) has been prepared and characterized by several spectroscopic techniques to verify its structure and purity. Sn(IV)-NCP shows a red shift in both the Soret and Q bands compared to the free base NCTPP. The last Q band appears in the NIR region.
View Article and Find Full Text PDFJ Inorg Biochem
January 2025
Department of Chemistry, University of Kentucky, 506 Library Drive, 146 Chemistry-Physics Building, Lexington, KY 40506-0055, USA. Electronic address:
ChemMedChem
November 2024
Department of Chemistry, Gauhati University, Guwahati, Assam, 781014, India.
In recent years, Sn(IV) porphyrins have proven to be excellent choice as photosensitizers for photodynamic therapy. This work reports the synthesis, characterization and photodynamic activity of four high-valent fluorinated Sn(IV) porphyrins having different numbers of F-atoms in the peripheral of meso-phenyl groups viz. (Dichloro)meso-tetrakis(4-fluorophenylporphyrinato)stannic(IV), [Sn(IV)FTPP(Cl)] or Sn1; (Dichloro)meso-tetrakis(2,4-difluorophenylporphyrinato)stannic(IV), [Sn(IV)2,4-FTPP(Cl)] or Sn2; (Dichloro)meso-tetrakis(2,6-difluorophenylporphyrinato)stannic(IV), [Sn(IV)2,6-FTPP(Cl)] or Sn3 and (Dichloro)meso-tetrakis(4-trifluoromethylphenylporphyrinato)stannic(IV), [Sn(IV)CFTPP(Cl)] or Sn4.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2024
Key Laboratory of Advanced Materials (MOE), Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
Polyacrylamide (PAM) hydrogel is hard to enhance through coordination bonds because amide groups rarely coordinate with metal ions strongly in an aqueous solution. It is known that the aqueous solution of ZrOCl.8HO can be strongly acidic depending on its concentration.
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